Canonical Allele Identifier: CA355715604

Gene: AHSG

Linked Data

• MyVariant Identifiers: chr3:g.186338435G>T (hg19) ; chr3:g.186620646G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186620646G>T , CM000665.2:g.186620646G>T	GRCh38
NC_000003.11:g.186338435G>T , CM000665.1:g.186338435G>T	GRCh37
NC_000003.10:g.187821129G>T	NCBI36
NG_011436.1:g.12586G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.820G>T MANE Select	ENSP00000393887.2:p.Asp274Tyr
ENST00000273784.5:c.823G>T	ENSP00000273784.5:p.Asp275Tyr
ENST00000411641.6:c.820G>T	ENSP00000393887.2:p.Asp274Tyr
NM_001622.2:c.820G>T	NP_001613.2:p.Asp274Tyr
NM_001354571.1:c.823G>T	NP_001341500.1:p.Asp275Tyr
NM_001354572.1:c.817G>T	NP_001341501.1:p.Asp273Tyr
NM_001354573.1:c.736G>T	NP_001341502.1:p.Asp246Tyr
NM_001622.3:c.820G>T	NP_001613.2:p.Asp274Tyr
NM_001622.4:c.820G>T MANE Select	NP_001613.2:p.Asp274Tyr
NM_001354571.2:c.823G>T	NP_001341500.1:p.Asp275Tyr
NM_001354572.2:c.817G>T	NP_001341501.1:p.Asp273Tyr
NM_001354573.2:c.736G>T	NP_001341502.1:p.Asp246Tyr